Gene
slc35b2
- ID
- ZDB-GENE-050213-1
- Name
- solute carrier family 35 member B2
- Symbol
- slc35b2 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Is predicted to enable 3'-phosphoadenosine 5'-phosphosulfate transmembrane transporter activity. Acts upstream of or within several processes, including osteoblast differentiation; proteoglycan biosynthetic process; and retinal ganglion cell axon guidance. Predicted to be located in membrane. Predicted to be integral component of membrane. Orthologous to human SLC35B2 (solute carrier family 35 member B2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Clément et al., 2008
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 17 figures from 8 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| hypomyelinating leukodystrophy 26 | Alliance | Leukodystrophy, hypomyelinating, 26, with chondrodysplasia | 620269 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
| Protein | Length |
|---|---|
|
UniProtKB:Q6P101
|
435 |
| Type | Name | Length (nt) | Analysis |
|---|---|---|---|
| mRNA |
slc35b2-201
(1)
|
3321 nt |
Interactions and Pathways
No data available
Plasmids
No data available